Remote Clinical Science Manager – Trials & Strategy

Aequor

Basking Ridge (NJ)

À distance

USD 90 000 - 130 000

Plein temps

Il y a 5 jours
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Résumé du poste

Aequor in the United States is seeking a Clinical Scientist to draft development plans, protocols, ICFs, and study-level documentation under the guidance of the CSL and Medical Monitor. The role includes data cleaning, literature reviews, and collaboration with a global study team.

You will work with Biostatistics, Data Management, and Clinical Operations to shape SAPs, SDV plans, and CSR outputs, contributing to successful study execution in a fast-paced environment.

Qualifications

  • 1-3 years of clinical experience with advanced degree preferred.
  • 3+ years of clinical experience with Bachelor's degree required.
  • Experience in oncology trials and cross-functional collaboration valued.

Responsabilités

  • Study Strategy: draft development plans, protocols, and SDV-related documents under CSL/Medical Monitor guidance.
  • Study Planning and Execution: support study design, risk identification, and contingency planning across teams.
  • Study outputs: review data quality listings, contribute to SAP updates and CSR preparation.
  • External collaboration: interact with CROs, AROs, KOLs, and internal subject-matter experts.
  • Literature review: perform reviews related to new indications for Life Cycle Management.

Connaissances

Strategic Thinking
Clinical Trials Knowledge
Influencing Skills
Scientific Knowledge
Therapeutic Expertise
Critical Thinking
Project Management
Communication Skills

Formation

Bachelor's degree
PharmD or PhD preferred

Description du poste

Aequor in the United States is seeking a Clinical Scientist to draft development plans, protocols, ICFs, and study-level documentation under the guidance of the CSL and Medical Monitor. The role includes data cleaning, literature reviews, and collaboration with a global study team.

You will work with Biostatistics, Data Management, and Clinical Operations to shape SAPs, SDV plans, and CSR outputs, contributing to successful study execution in a fast-paced environment.

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